NDC 51407-272 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51407-272

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205087
Marketed since
September 23, 2015
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51407-272-101000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)Aug 22, 2019

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